Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Cholinergic Antagonists: Chemistry and Structure-Activity Relationship01:29

Cholinergic Antagonists: Chemistry and Structure-Activity Relationship

2.2K
Cholinergic antagonists bind to cholinergic receptors and limit the effects of acetylcholine and other cholinergic agonists. Based on the specific cholinergic receptor affinity, these antagonists are classified as muscarinic or nicotinic. Anticholinergics interrupt parasympathetic innervations while sympathetic innervations remain uninterrupted. Muscarinic antagonists are also called 'muscarinic antagonists', 'antimuscarinics', or 'parasympatholytics'. Nicotinic...
2.2K
Adrenergic Agonists: Chemistry and Structure-Activity Relationship01:16

Adrenergic Agonists: Chemistry and Structure-Activity Relationship

3.0K
Adrenergic agonists' structure-activity relationship (SAR) determines their selectivity and efficacy. These agonists comprise a phenylethylamine moiety with an aromatic ring and an ethylamine side chain.
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of...
3.0K
Direct-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship01:22

Direct-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship

953
Cholinergic agonists or cholinomimetics mimic the action of acetylcholine to stimulate the parasympathetic nervous system. They are categorized into direct-acting and indirect-acting agents. The direct-acting cholinergic drugs induce the parasympathetic response by directly binding to the muscarinic or nicotine receptors. In comparison, the indirect-acting cholinergic drugs prevent acetylcholine hydrolysis, indirectly contributing to the extended parasympathetic response.
The direct-acting...
953
Amines: Introduction01:07

Amines: Introduction

4.4K
Amines are organic derivatives of ammonia. They are formed by replacing one or more ammonia protons with alkyl or aryl groups. Depending upon the number of organyl groups bonded to nitrogen, amines are classified as primary, secondary, or tertiary. Primary amines have one organyl group attached to the nitrogen atom, while secondary and tertiary amines have two and three organyl groups attached to the nitrogen atom, respectively.
4.4K
Physical Properties of Amines01:26

Physical Properties of Amines

3.1K
Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
3.1K
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship01:29

Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship

556
Indirect-acting cholinergic agonists are agents that interact with the acetylcholinesterase enzyme in the synaptic cleft, preventing the breakdown of acetylcholine into choline and acetate. Consequently, the concentration of acetylcholine in the synaptic cleft increases. These agonists can be classified into reversible and irreversible inhibitors based on their duration of action.
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
556

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

The scramblase anoctamin 9 controls the immune response in lymphocytes.

Cellular and molecular life sciences : CMLS·2026
Same author

Case Report of Pediatric HPCA-Associated Dystonia: Analysis of Ca<sup>2+</sup> and K<sup>+</sup> Channel Dynamics and Experience With Pallidal Deep Brain Stimulation.

Pediatric neurology·2025
Same author

Anoctamin 9 determines Ca<sup>2+</sup> signals during activation of T-lymphocytes.

Frontiers in immunology·2025
Same author

Global functional genomics reveals GRK5 as a cystic fibrosis therapeutic target synergistic with current modulators.

iScience·2025
Same author

Perinatal dysfunction of innate immunity in cystic fibrosis.

Science translational medicine·2025
Same author

Dystonia caused by ANO3 variants is due to attenuated Ca<sup>2+</sup> influx by ORAI1.

BMC medicine·2025

相关实验视频

Updated: Jun 28, 2025

Identification of Hemolytic and Phospholipase Activity in Crude Extracts from Sea Anemones by Straightforward Bioassays
12:12

Identification of Hemolytic and Phospholipase Activity in Crude Extracts from Sea Anemones by Straightforward Bioassays

Published on: March 29, 2022

2.8K

亚诺胺:结构和功能

Rainer Schreiber1, Jiraporn Ousingsawat1, Karl Kunzelmann1

  • 1Physiological Institute, University of Regensburg, University street 31, D-93053 Regensburg, Germany.

Cell calcium
|April 20, 2024
PubMed
概括
此摘要是机器生成的。

离子通道称为阿诺胺 (ANO),特别是ANO1,调节腺体和表皮中的离子运输. 突出了它们在健康和患有脏,包括多囊脏病中的作用.

关键词:
没有了,没有了,没有了.

更多相关视频

Harvesting and Cryo-cooling Crystals of Membrane Proteins Grown in Lipidic Mesophases for Structure Determination by Macromolecular Crystallography
18:45

Harvesting and Cryo-cooling Crystals of Membrane Proteins Grown in Lipidic Mesophases for Structure Determination by Macromolecular Crystallography

Published on: September 2, 2012

25.0K
Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET
12:07

Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET

Published on: October 9, 2021

3.4K

相关实验视频

Last Updated: Jun 28, 2025

Identification of Hemolytic and Phospholipase Activity in Crude Extracts from Sea Anemones by Straightforward Bioassays
12:12

Identification of Hemolytic and Phospholipase Activity in Crude Extracts from Sea Anemones by Straightforward Bioassays

Published on: March 29, 2022

2.8K
Harvesting and Cryo-cooling Crystals of Membrane Proteins Grown in Lipidic Mesophases for Structure Determination by Macromolecular Crystallography
18:45

Harvesting and Cryo-cooling Crystals of Membrane Proteins Grown in Lipidic Mesophases for Structure Determination by Macromolecular Crystallography

Published on: September 2, 2012

25.0K
Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET
12:07

Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET

Published on: October 9, 2021

3.4K

科学领域:

  • 细胞生物学 细胞生物学
  • 身体生理学 身体生理学

背景情况:

  • 亚诺胺 (TMEM16蛋白质) 是Ca2+激活的脂混合酶和离子通道.
  • 亚诺胺1 (ANO1) 是一种Ca2+激活的阳离子选择性通道,与酶ANO6和其他亚诺胺一起表达.
  • ANO1在唾液和胰腺,呼吸道和肠道上皮质中发挥作用,通常支持CFTR功能.

研究的目的:

  • 综述阿诺胺的多样性功能,重点关注ANO1.
  • 探索ANO1在健康和病理条件,特别是功能和疾病中的作用.
  • 讨论其他表皮性无胺的潜在功能.

主要方法:

  • 文献审查的阿诺胺功能.
  • 分析ANO1在各种上皮组织 (腺体,呼吸道,肠道,脏) 中的作用.
  • 讨论ANO1和ANO6参与诸如多囊性病等病理状况.

主要成果:

  • 在腺体中,ANO1作为Cl-通道,在呼吸道和肠道中支持CFTR.
  • 在脏中,ANO1参与酸分泌,蛋白质再吸收和HCO3-分泌.
  • 在多囊性病中,ANO1和ANO6被上调,可能导致的增殖和生长.

结论:

  • 亚诺胺,特别是ANO1,在表皮离子运输和细胞过程中起着关键作用.
  • 在健康和病态状态之间,ANO1的功能有很大差异,对脏疾病有影响.
  • 需要进行进一步的研究,以充分阐明其他上皮性阿诺胺的功能.